85044-77-5 Usage
Derivative of imidazole
A modified version of the imidazole molecule, which is a naturally occurring organic compound with potential antimicrobial and antifungal properties.
Nitro group attachment
A nitro group (-NO2) is attached to the imidazole ring, which may contribute to the compound's biological activity and potential therapeutic applications.
Phenylsulfonyl group attachment
A phenylsulfonyl group (C6H5SO2-) is attached to the nitrogen atom in the imidazole ring, further enhancing the compound's potential biological activity.
Antimicrobial potential
Due to its imidazole structure, this compound has the potential to be used as an antimicrobial agent, targeting bacteria and other microorganisms.
Antifungal potential
The imidazole structure also provides antifungal properties, making it a potential candidate for treating fungal infections.
Need for further research
Despite its potential applications, more research and studies are required to fully understand the pharmacological and biochemical properties of 1-methyl-5-nitro-4-(phenylsulfonyl)-1H-imidazole.
Check Digit Verification of cas no
The CAS Registry Mumber 85044-77-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,0,4 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 85044-77:
(7*8)+(6*5)+(5*0)+(4*4)+(3*4)+(2*7)+(1*7)=135
135 % 10 = 5
So 85044-77-5 is a valid CAS Registry Number.
85044-77-5Relevant articles and documents
Nucleophilic Displacements of Imidazoles.II Displacements of Halogen by S-Nucleophiles and Displacements of Mesyl Groups Activated by Nitro; Oxidation of Imidazolethiols
Kulkarni, Surendra,Grimmett, M. Ross
, p. 1415 - 1425 (2007/10/02)
In basic medium arylthiols displace bromo and iodo groups activated by nitro substituents in 5(4)-halo-4(5)-nitroimidazoles.The bromo compounds are slightly more reactive than the iodo analogues.Substituents at C5 are more readily displaced than those at
